Supplementary Figure 3

Similar documents
Cao, J, K Schneeberger, S Ossowski, et al Whole genome sequencing of multiple Arabidopsis thaliana populations. Nat Genet 43:

Supplementary Figure 1. Number of CC- and TIR- type NBS- LRR genes and presence of mir482/2118 on sequenced plant genomes.

SUPPLEMENTARY INFORMATION

Bioinformatics tools to analyze complex genomes. Yves Van de Peer Ghent University/VIB

Evaluation of Genome Sequencing Quality in Selected Plant Species Using Expressed Sequence Tags

SUPPLEMENTARY INFORMATION

Supplemental Table 1. Primers used for cloning and PCR amplification in this study

Genome-wide discovery of G-quadruplex forming sequences and their functional

Eud! Mag! Chl! Cer! Mon! outgroup! g 88. Eud! Cer! <50. Chl! Mag! Mon! outgroup! Eud! Mon! Cer! Mag! Chl! outgroup!

Supplementary Material

Identification of new members of the MAPK gene family in plants shows diverse conserved domains and novel activation loop variants

SUPPLEMENTARY INFORMATION

AtTIL-P91V. AtTIL-P92V. AtTIL-P95V. AtTIL-P98V YFP-HPR

Integrating Phylogenetic and Network Approaches to Study Gene Family Evolution: The Case of the AGAMOUS Family of Floral Genes

Supplemental Figure 1. Comparison of Tiller Bud Formation between the Wild Type and d27. (A) and (B) Longitudinal sections of shoot apex in wild-type

Miloš Duchoslav and Lukáš Fischer *

Supplemental Data. Yang et al. (2012). Plant Cell /tpc

Supplementary Information for: The genome of the extremophile crucifer Thellungiella parvula

** LCA LCN PCA

Potato Genome Analysis

The evolution of WRKY transcription factors

Supplemental Data. Perea-Resa et al. Plant Cell. (2012) /tpc

Evolution of tonoplast P-ATPase transporters involved in vacuolar acidification

Plant Genome Sequencing

Agave Genomics in Support

Browsing Genomic Information with Ensembl Plants

Phylogenetic Comparison of F-Box (FBX) Gene Superfamily within the Plant Kingdom Reveals Divergent Evolutionary Histories Indicative of Genomic Drift

Supplementary Information

Cryopreservation of syn seeds

Regulatory Change in YABBY-like Transcription Factor Led to Evolution of Extreme Fruit Size during Tomato Domestication

gi (NCBI databse: ES frame +2 (NCBI: databse

Jill M Duarte 1, P Kerr Wall 1,5, Patrick P Edger 2, Lena L Landherr 1, Hong Ma 1,4, J Chris Pires 2, Jim Leebens-Mack 3, Claude W depamphilis 1*

SUPPLEMENTARY MATERIAL SUPPLEMENTARY TABLES

South Green Bioinformatics activities at CIRAD

Supplemental Figure 1. Comparisons of GC3 distribution computed with raw EST data, bi-beta fits and complete genome sequences for 6 species.

Supplementary Figure 1

D. Incorrect! That is what a phylogenetic tree intends to depict.

08/21/2017 BLAST. Multiple Sequence Alignments: Clustal Omega

Impact of recurrent gene duplication on adaptation of plant genomes

Genome-Wide Identification of NBS-Encoding Resistance Genes in Sunflower (Helianthus annuus L.)

USDA-DOE Plant Feedstock Genomics for Bioenergy

Systematic Analysis and Comparison of Nucleotide-Binding Site Disease Resistance Genes in a Diploid Cotton Gossypium raimondii

Stage 1: Karyotype Stage 2: Gene content & order Step 3

Supplementary Information

Molecular Population Genetics of Arabidopsis thaliana Ferulate-5-Hydroxylase and Flavanone-3-Hydroxylase Genes

Research Article Identification of Immune Related LRR-Containing Genes in Maize (Zea mays L.) by Genome-Wide Sequence Analysis

Nature Genetics: doi: /ng Supplementary Figure 1. The phenotypes of PI , BR121, and Harosoy under short-day conditions.

Origin and diversification of leucine-rich repeat receptor-like protein kinase (LRR-RLK) genes in plants

Paleo-evolutionary plasticity of plant disease resistance genes

Journal of Integrative Agriculture 2017, 16(5): Available online at ScienceDirect

THEORY. Based on sequence Length According to the length of sequence being compared it is of following two types

Genome-wide analysis of TCP family in tobacco

Dr. Amira A. AL-Hosary

Intraspecific gene genealogies: trees grafting into networks

Variation, Evolution, and Correlation Analysis of C+G Content and Genome or Chromosome Size in Different Kingdoms and Phyla

Host_microbe_PPI - R package to analyse intra-species and interspecies protein-protein interactions in the model plant Arabidopsis thaliana

Genomics and Bioinformatics Resources for Crop Improvement

Genome-wide analysis of nucleotide-binding site disease resistance genes in Medicago truncatula

Genome-wide Identification of Lineage Specific Genes in Arabidopsis, Oryza and Populus

Supplemental Data. Fernández-Calvo et al. Plant Cell. (2011) /tpc

"Nothing in biology makes sense except in the light of evolution Theodosius Dobzhansky

Supporting Information

Additional file 10. Classification of Pac sequences based on maximum-likelihood (ML) phylogenetic analyses. Analyses were performed on the same

Comparative Protein Modeling of Superoxide Dismutase Isoforms in Maize.

Muñoz-Clares et al. BMC Plant Biology 2014, 14:149

Amira A. AL-Hosary PhD of infectious diseases Department of Animal Medicine (Infectious Diseases) Faculty of Veterinary Medicine Assiut

Research Article mir156- and mir171-binding Sites in the Protein-Coding Sequences of Several Plant Genes

Concerted divergence after gene duplication in Polycomb Repressor. complexes

A greedy, graph-based algorithm for the alignment of multiple homologous gene lists

Genome-Wide Computational Prediction and Analysis of Core Promoter Elements across Plant Monocots and Dicots

Supporting Information

Evolution by duplication: paleopolyploidy events in plants reconstructed by deciphering the evolutionary history of VOZ transcription factors

Bioinformatics tools for phylogeny and visualization. Yanbin Yin

Nature Genetics: doi: /ng Supplementary Figure 1. ssp mutant phenotypes in a functional SP background.

Research Article Genome-Wide Identification, Evolutionary, and Expression Analyses of Histone H3 Variants in Plants

Slovene Plant Gene Bank (SPGB) and Genetic Resources Programme

Anatomy of a tree. clade is group of organisms with a shared ancestor. a monophyletic group shares a single common ancestor = tapirs-rhinos-horses

Phylogeny and systematics. Why are these disciplines important in evolutionary biology and how are they related to each other?

Other Supplemenary Materials for this manuscript includes the following:

Identification and characterization of the bzip transcription factor involved in zinc homeostasis in cereals

Evolution of the Rdr1 TNL-cluster in roses and other Rosaceous species

training workshop 2015

Levels of genetic variation for a single gene, multiple genes or an entire genome

The Solute Accumulation: The Mechanism for Drought Tolerance in RD23 Rice (Oryza sativa L) Lines

The Journal of Animal & Plant Sciences, 28(5): 2018, Page: Sadia et al., ISSN:

Phylogenetic analyses. Kirsi Kostamo

Enduring Understanding: Change in the genetic makeup of a population over time is evolution Pearson Education, Inc.

SUPPLEMENTARY INFORMATION

A computational analysis of Salt Overly Sensitive 1 homologs in halophytes and glycophytes

Name: Class: Date: ID: A

Neofunctionalization within the Omp85 protein superfamily during

Whole genome duplication events in plant evolution reconstructed and predicted using myosin motor proteins

Cladistics and Bioinformatics Questions 2013

biology Exploiting a Reference Genome in Terms of Duplications: The Network of Paralogs and Single Copy Genes in Arabidopsis thaliana

MULTIPLE SEQUENCE ALIGNMENT FOR CONSTRUCTION OF PHYLOGENETIC TREE

Supporting Information Figs S1 S7

Consensus Methods. * You are only responsible for the first two

I. Short Answer Questions DO ALL QUESTIONS

Assessment of phylogenetic signal in the germination ability of broomrape (Phelipanche ramosa) on Brassicaceae hosts

Warm Up. Explain how a mutation can be detrimental in one environmental context and beneficial in another.

Transcription:

Supplementary Figure 3 7.0 Col Kas-1 Line FTH1A 8.4 F3PII3 8.9 F26H11 ATQ1 T9I22 PLS8 F26B6-B 9.6 F27L4 9.81 F27D4 9.92 9.96 10.12 10.14 10.2 11.1 0.5 Mb T1D16 Col % RGR 83.3 101 227 93.5 75.9 132 90 375 70.9 300 84.1 297 574 609 1.2 76.32 70.3 578 0 289 535 1.12 8.0 L128 20.6 Supplementary Figure 3. Fine mapping of ATQ1. Genotype and As(V) tolerance phenotype, determined as %RGR, in selected lines from a NIL128 x Col gl-1 (Col) F 2 population. The recombination breakpoints at the FTH1A and T1D16 interval are depicted; Kas-1 (red), Col gl-1 (Col; green). ATQ1 is located between markers F26H11 and T9I22.

Supplementary Figure 5 Supplementary Figure 5. Phylogenetic relationships among rhodanase proteins. Neighbor-Joining tree including 49 sequences from 31 plant species selected by the highest homology to the rhodanase encoded by AtARQ1 gene (At2g21045). They correspond to three Arabidopsis thaliana proteins (AtARQ1, At5g66170 and At5g66040), a pair of proteins from each of 16 plant species (indicated with numbers 1 or 2 close to species names) and a single protein from each of 14 other plants. In addition, 9 ACR2 like proteins are included from protista, algae and plants. The bootstrap consensus tree inferred from 10000 replicates is taken to represent the evolutionary history of the taxa analyzed. The evolutionary distances were computed using the Poisson correction method and are in the units of the number of amino acid substitutions per site. The analysis involved 58 amino acid sequences. All ambiguous positions were removed for each sequence pair. There were a total of 200 positions in the final dataset. Evolutionary analysis was conducted in MEGA6 51. Sequence accession numbers are: Arabidopsis thaliana AtARQ1 (At2g21045): AAP37665; Arabidopsis thaliana AT5G66040: AAN38701; Arabidopsis thaliana AT5G66170: AAM10268; Arabidopsis lyrata 1: 899363; Arabidopsis lyrata 2: 496998; Thellungiella halophila 1: Thhalv10022902m; Thellungiella halophila 1: Thhalv10005118m; Capsella rubella 1: Carubv10025520m; Capsella rubella 2: Carubv10028451m; Brassica rapa 1: Bra002059; Brassica rapa 2: Bra012056; Carica papaya 1: supercontig 37.162; Carica papaya 2: supercontig 6.271; Cucumis sativus 1: CucsArabidopsis234370; Cucumis sativus 2: CucsArabidopsis044010; Prunus persica 1: ppa024101; Prunus persica 2: ppa011976; Malus domestica: MDP0000433388; Mimulus guttatus: mgv1a018856; Vitis vinifera 1: GSVIVG01018758001; Vitis vinifera 2: GSVIVG01018760001; Manihot esculenta: cassava4.1 017198; Citrus sinensis 1: orange1.1g041947m; Citrus sinensis 2: orange1.1g032621m; Citrus clementina: Ciclev10026690m; Setaria italica: Si031418m; Aquilegia coerulea: Aquca_006_00217.1; Eucalyptus grandis 1: Eucgr.E01127.1; Eucalyptus grandis 2: Eucgr.L00782.1; Solanum tuberosum: PGSC0003DMG400003573; Solanum lycopersicum: Solyc02g083730.2.1; Medicago truncatula 1: Medtr2g017630.1; Medicago truncatula 2: Medtr8g075420.1; Glycine max 1: Glyma12g02040.1; Glycine max 2: Glyma01g37010.1; Phaseouls vulgaris: Phvul.011G020400; Gossypium raimondii 1: Gorai.013G141700.1; Gossypium raimondii 2: Gorai.007G049000.3; Populus trichocarpa 1: Potri.014G131300.1; Populus trichocarpa 2: Potri.005G111200.2; Fragaria vesca: mrna24304.1-v1.0-hybrid; Theobroma cacao: Thecc1EG032968t1; Brachypodium distachyon: Bradi3g00377.1; Oriza sativa 1: Os04g17660.1; Oriza sativa 2: Os02g01220.1; Panicum virgatum: Pavirv00038676m; Sorghum bicolor 1: Sb06g003340; Sorghum bicolor 2: Sb04g000410; Zea mays: AC204711.3 FG003; Saccharomyces cerevisae ACR2: NP 015526; Leishmania major ACR2: AAS73185; Gossypium arboreum ACR2: AW666950; Oriza sativa ACR2: BE039986; Chlamydomonas reinhardtii ACR2: AW661050; Arabidopsis thaliana ACR2 AT5G03455: AAO39886; Pteris vittata ACR2: ADP20951; Holcus lanatus ACR2: AY704470; Zea mays ACR2: AY108501.

Supplementary Figure 7 a Col-0 ATGTATACATATTCTCTCCTCAACCTTTCTCATTGCAGAAGACAAACCAGAAAGAAAAGAAAAACAGATCACACCGAAGGCTTTCTCATGGAGGAAACAA Kas-1 ATG-ATACATATCCTCTCTTCAACCTTTCTCATTGCAAAAGACATACCAGAA-----AGAAAAACAGATCAAACCGAAGGCTTTCTCATGGAGGAAACAA Col-0 AACCAAAGACCGTTGAAGATGTTGAGACCGTTGATGTTTATACAGCTAAAGGCTTTCTTAGTACTGGTCACCGATATCTCGACGTAAGGACAAATGAAGA Kas-1 AACCAAAGACCGTTGAAGATGTTGAGACCGTTGATATTTATACAGCTAAAGGCTTTCTTAGTACTGGTCACCGATATCTCGACGTAAGGACAAGTGAAGA Col-0 ATTTGCCAAGAGTCATGTTGAGGAGGCTTTGAACATTCCTTATATGTTCAAAACAGATGAAGGTAGGGTTATAAATCCTGATTTCCTTTCTCAAGTGGCA Kas-1 ATTTGCCAAGAGTCATGTTGAGGAGGCTTTGAACATTCCTTATATGTTCCAAACAGATGAAGGTAGGGTTATAAATCCTGATTTCCTTTCTCAAGTGGCA Col-0 TCGGTTTGCAAGAAAGATGAACATTTGATCGTGGCTTGTAACGCTGGAGGAAGAGGAAGTCGTGCTTGCGTTGATCTTCTTAACGAGGGGTACGACCATG Kas-1 TCGGTTTGCAAGAAAGATGAACATTTGATCGTGGCTTGTAACGCTGGAGGAAGAGGAAGTCGTGCTTGCGTTGATCTTCTCAACGAGGGGTACGACCATG * Col-0 TGGCTAACATGGGGGGAGGCTACTCGGCTTGGGTTGACGCTGGATTCGCCGGGGACAAACCCCCGGAAGACCTCAAGATTGCTTGCAAGTTCAGGCCAAA Kas-1 TGGCTAACATGGGGGGAGGCTACTCGGCTTGGGTTGACGCTGGATTCGCCGGGGACAAACCCCCGGGAGACCTCAAGATTGCTTGCAAGTTCAGGCCAAA Col-0 GGAAAACTAA Kas-1 GGAAAACTAA b Bur-0 Chi-0 Col-0 Lm-2 Kz-2 Bay-0 Pi-0 Yeg-1 Sav-0 Ct-1 Fuk-0 Es-0 A.lyrata Kas-1 Fei-0 Edi-0 Ll-0 Ri-0 Shak-0 Tsu-1 kondara c 0.01 Supplementary Figure 7. Col-0 and Kas-1 define two haplogroups for the AtARQ1 gene in Arabidopsis thaliana. (a) Nucleotide diversity between Col-0 and Kas-1 AtARQ1 coding sequence. Compensatory indels and single nucleotide polymorphisms in Col-0 (green) and Kas-1 (red). *synonymous mutation. (b) Phylogram constructed using Clustal-W of AtARQ1 coding sequences from 20 Arabidopsis accessions and Arabidopsis lyrata. (c) Geographic distribution of Arabidopsis accessions used, classified by Col-0 or Kas-1 haplogroup.